WNT10B, Wnt family member 10B, 7480

N. diseases: 90; N. variants: 23
Disease: Polydactyly ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0152427
Disease: Polydactyly
Polydactyly 		0.110 GeneticVariation disease BEFREE Based on this classification and a review of all previously reported cases, we demonstrate that SHFM6 caused by WNT10B pathogenic variants have the following characteristics: more severe feet defects (compared to the hand defects), polydactyly, severe flexion digital contractures, and phalangeal dysplasia. 31421290 2020
CUI: C0152427
Disease: Polydactyly
Polydactyly 		0.110 GeneticVariation disease CLINVAR